Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg3 |
A |
G |
5: 105,116,081 (GRCm39) |
L251S |
probably damaging |
Het |
Acsbg1 |
C |
T |
9: 54,535,843 (GRCm39) |
S53N |
unknown |
Het |
Adamts18 |
A |
G |
8: 114,439,855 (GRCm39) |
C913R |
probably damaging |
Het |
Adck5 |
C |
A |
15: 76,479,588 (GRCm39) |
Y524* |
probably null |
Het |
Adgrv1 |
G |
T |
13: 81,251,443 (GRCm39) |
Q6225K |
possibly damaging |
Het |
Ahr |
T |
C |
12: 35,554,016 (GRCm39) |
N701S |
probably damaging |
Het |
Apc |
T |
C |
18: 34,447,261 (GRCm39) |
C1386R |
probably damaging |
Het |
Bbs1 |
A |
G |
19: 4,956,182 (GRCm39) |
S38P |
probably benign |
Het |
Celsr1 |
G |
T |
15: 85,862,933 (GRCm39) |
C1366* |
probably null |
Het |
Cep290 |
A |
C |
10: 100,375,919 (GRCm39) |
H1424P |
probably benign |
Het |
Clcn3 |
C |
T |
8: 61,386,119 (GRCm39) |
R311K |
possibly damaging |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Dhx9 |
A |
G |
1: 153,334,152 (GRCm39) |
Y1002H |
probably damaging |
Het |
Dnah8 |
C |
T |
17: 30,876,947 (GRCm39) |
T533I |
probably damaging |
Het |
Ermard |
T |
C |
17: 15,279,724 (GRCm39) |
S505P |
probably benign |
Het |
Fbxw17 |
G |
A |
13: 50,579,680 (GRCm39) |
D166N |
probably damaging |
Het |
Fmo3 |
T |
C |
1: 162,785,901 (GRCm39) |
K363R |
possibly damaging |
Het |
Frey1 |
C |
A |
2: 92,213,817 (GRCm39) |
P68Q |
probably damaging |
Het |
Gadd45gip1 |
A |
T |
8: 85,558,980 (GRCm39) |
R21W |
probably damaging |
Het |
Galnt4 |
A |
G |
10: 98,945,826 (GRCm39) |
N517S |
probably benign |
Het |
Ganc |
T |
A |
2: 120,264,273 (GRCm39) |
W409R |
probably damaging |
Het |
Glrx3 |
T |
C |
7: 137,060,920 (GRCm39) |
S185P |
probably damaging |
Het |
Gm49368 |
T |
C |
7: 127,712,414 (GRCm39) |
S853P |
probably damaging |
Het |
Gtf3c2 |
A |
C |
5: 31,325,611 (GRCm39) |
L443V |
probably damaging |
Het |
Gxylt2 |
A |
T |
6: 100,781,489 (GRCm39) |
Q388L |
probably benign |
Het |
Ifit3b |
A |
T |
19: 34,589,955 (GRCm39) |
D377V |
possibly damaging |
Het |
Ints5 |
A |
G |
19: 8,874,168 (GRCm39) |
D709G |
probably benign |
Het |
Lyst |
A |
G |
13: 13,844,450 (GRCm39) |
E1880G |
probably benign |
Het |
Mep1a |
C |
T |
17: 43,790,065 (GRCm39) |
S428N |
probably benign |
Het |
Mllt6 |
T |
C |
11: 97,567,790 (GRCm39) |
L739P |
probably damaging |
Het |
Mlst8 |
T |
C |
17: 24,695,031 (GRCm39) |
Y284C |
probably damaging |
Het |
Mmel1 |
T |
C |
4: 154,956,111 (GRCm39) |
M1T |
probably null |
Het |
Muc5ac |
C |
T |
7: 141,363,120 (GRCm39) |
P2144S |
unknown |
Het |
Myh4 |
T |
C |
11: 67,131,756 (GRCm39) |
V72A |
probably benign |
Het |
Naa15 |
T |
A |
3: 51,377,395 (GRCm39) |
|
probably null |
Het |
Nlrc5 |
A |
G |
8: 95,248,028 (GRCm39) |
|
probably null |
Het |
Nme8 |
T |
A |
13: 19,835,145 (GRCm39) |
M514L |
probably benign |
Het |
Nudt9 |
C |
A |
5: 104,194,946 (GRCm39) |
S14* |
probably null |
Het |
Optn |
G |
A |
2: 5,059,461 (GRCm39) |
T19I |
probably benign |
Het |
Or11h23 |
A |
T |
14: 50,948,215 (GRCm39) |
I143F |
possibly damaging |
Het |
Or13a24 |
T |
C |
7: 140,154,159 (GRCm39) |
F31S |
probably damaging |
Het |
Osbpl8 |
T |
A |
10: 111,112,370 (GRCm39) |
L495* |
probably null |
Het |
Panx2 |
T |
C |
15: 88,951,973 (GRCm39) |
S147P |
possibly damaging |
Het |
Pclo |
T |
A |
5: 14,730,630 (GRCm39) |
V3044D |
unknown |
Het |
Pcnt |
T |
C |
10: 76,258,642 (GRCm39) |
K608E |
probably benign |
Het |
Pde7a |
T |
A |
3: 19,281,909 (GRCm39) |
N447I |
probably damaging |
Het |
Peli2 |
G |
T |
14: 48,517,491 (GRCm39) |
C186F |
not run |
Het |
Pgm5 |
A |
G |
19: 24,705,215 (GRCm39) |
F433L |
probably benign |
Het |
Plce1 |
G |
A |
19: 38,736,877 (GRCm39) |
V1588I |
probably benign |
Het |
Plin4 |
T |
A |
17: 56,409,413 (GRCm39) |
H1295L |
probably benign |
Het |
Poli |
T |
C |
18: 70,658,590 (GRCm39) |
E134G |
probably benign |
Het |
Pramel11 |
T |
A |
4: 143,624,371 (GRCm39) |
D42V |
probably benign |
Het |
Ptprq |
T |
A |
10: 107,479,839 (GRCm39) |
I1144F |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 23,024,977 (GRCm39) |
T1738S |
probably damaging |
Het |
Pxdc1 |
A |
G |
13: 34,836,267 (GRCm39) |
L51P |
probably damaging |
Het |
Rabepk |
C |
T |
2: 34,669,308 (GRCm39) |
G362S |
probably damaging |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Rhd |
T |
A |
4: 134,611,820 (GRCm39) |
|
probably null |
Het |
Rpp14 |
T |
C |
14: 8,090,453 (GRCm38) |
S126P |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,506,536 (GRCm39) |
C1451Y |
probably damaging |
Het |
Sdr39u1 |
G |
A |
14: 56,135,191 (GRCm39) |
R251* |
probably null |
Het |
Sephs2 |
G |
T |
7: 126,872,506 (GRCm39) |
P196T |
possibly damaging |
Het |
Slc22a16 |
T |
C |
10: 40,450,085 (GRCm39) |
Y195H |
possibly damaging |
Het |
Spg11 |
C |
A |
2: 121,899,361 (GRCm39) |
V1575F |
probably damaging |
Het |
Sqle |
C |
T |
15: 59,187,890 (GRCm39) |
S66L |
probably benign |
Het |
Tas2r124 |
T |
G |
6: 132,732,056 (GRCm39) |
W122G |
probably damaging |
Het |
Tex52 |
A |
T |
6: 128,361,921 (GRCm39) |
|
probably null |
Het |
Thoc1 |
T |
A |
18: 9,993,454 (GRCm39) |
C604* |
probably null |
Het |
Tmc3 |
T |
C |
7: 83,246,666 (GRCm39) |
S136P |
probably damaging |
Het |
Tmem212 |
T |
A |
3: 27,950,462 (GRCm39) |
T11S |
probably benign |
Het |
Ubn2 |
A |
G |
6: 38,468,727 (GRCm39) |
N1147S |
probably benign |
Het |
Uggt2 |
A |
G |
14: 119,312,759 (GRCm39) |
I350T |
probably damaging |
Het |
Ust |
A |
T |
10: 8,083,339 (GRCm39) |
Y346N |
probably damaging |
Het |
Vwa8 |
A |
G |
14: 79,335,740 (GRCm39) |
T1399A |
probably benign |
Het |
Zc3h18 |
G |
A |
8: 123,140,615 (GRCm39) |
R850Q |
unknown |
Het |
Zfp800 |
C |
A |
6: 28,244,193 (GRCm39) |
K257N |
probably damaging |
Het |
Zfp985 |
T |
A |
4: 147,667,331 (GRCm39) |
D66E |
probably benign |
Het |
|
Other mutations in Hcar2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00827:Hcar2
|
APN |
5 |
124,002,565 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01682:Hcar2
|
APN |
5 |
124,002,582 (GRCm39) |
missense |
probably benign |
0.09 |
R1450:Hcar2
|
UTSW |
5 |
124,002,813 (GRCm39) |
missense |
probably damaging |
0.98 |
R3014:Hcar2
|
UTSW |
5 |
124,002,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R3853:Hcar2
|
UTSW |
5 |
124,002,475 (GRCm39) |
missense |
probably benign |
|
R4539:Hcar2
|
UTSW |
5 |
124,002,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4720:Hcar2
|
UTSW |
5 |
124,002,752 (GRCm39) |
frame shift |
probably null |
|
R4784:Hcar2
|
UTSW |
5 |
124,002,513 (GRCm39) |
missense |
probably benign |
0.02 |
R4785:Hcar2
|
UTSW |
5 |
124,002,513 (GRCm39) |
missense |
probably benign |
0.02 |
R4886:Hcar2
|
UTSW |
5 |
124,003,260 (GRCm39) |
missense |
probably benign |
0.01 |
R5632:Hcar2
|
UTSW |
5 |
124,002,532 (GRCm39) |
missense |
probably benign |
0.17 |
R6211:Hcar2
|
UTSW |
5 |
124,003,017 (GRCm39) |
missense |
probably benign |
0.01 |
R6796:Hcar2
|
UTSW |
5 |
124,003,330 (GRCm39) |
missense |
probably benign |
0.00 |
R7341:Hcar2
|
UTSW |
5 |
124,002,541 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7483:Hcar2
|
UTSW |
5 |
124,002,861 (GRCm39) |
missense |
probably benign |
0.33 |
R7497:Hcar2
|
UTSW |
5 |
124,003,249 (GRCm39) |
missense |
probably benign |
0.04 |
R8429:Hcar2
|
UTSW |
5 |
124,003,538 (GRCm39) |
start gained |
probably benign |
|
R8984:Hcar2
|
UTSW |
5 |
124,002,571 (GRCm39) |
nonsense |
probably null |
|
R9192:Hcar2
|
UTSW |
5 |
124,003,354 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9384:Hcar2
|
UTSW |
5 |
124,002,597 (GRCm39) |
missense |
probably benign |
0.01 |
R9658:Hcar2
|
UTSW |
5 |
124,002,532 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Hcar2
|
UTSW |
5 |
124,003,269 (GRCm39) |
missense |
probably damaging |
1.00 |
|